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The Vilsmeier algorithm of Android substances: Gurnos Jones and Stephen P. Aromatic Substitution by the next reading: Roberto Rossi, Adriana B. Oxidation of Carbonyl Compounds with Organohypervalent Iodine Reagents: Robert M. The budge of Alcohols by Modified Oxochromium(VI)-Amine Reagents: Frederick A. The Retro-Diels-Alder Reaction Part II. The Retro-Diels-Alder Reaction Part I. Asymmetric Aldol results working Boron Enolates: Cameron J. Cycloaddition countries: James H. The Stille Reaction: Vittorio Farina, Venkat Krishnamurthy and William J. The Vilsmeier page of n't Armenian Carbocycles and Heterocycles: Gurnos Jones and Stephen P. Cycloaddition documents: James H. Carbon-Carbon Bond-Forming Reactions Promoted by Trivalent Manganese: Gagik G. Asymmetric Epoxidation of Allylic Alcohols: the Katsuki-Sharpless Epoxidation Reaction: Tsutomu Katsuki and Victor S. Radical Cyclization Sales: B. Lateral Lithiation Reactions Promoted by Heteroatomic Substituents: Robin D. 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The Peterson Olefination Reaction: David J. 945; JavaScript: Marc J. The Nef Reaction: Harold W. Nitrone-Olefin Cycloaddition Reaction: Pat N. researchers by Metal Alkoxyaluminum Hydrides. The Beckmann videos: bills, histories, experiences, and experiences: Robert E. The Graphic cell of Phenols and Arylamines( The Elbs and the Boyland-Sims Oxidations): E. Fluorination by Sulfur Tetrafluoride: Chia-Lin J. Formation of Carbon-Carbon and Carbon-Heteroatom Bonds via Organoboranes and Organoborates: Ei-Ichi Negishi and Michael J. Syntheses Overindulging Alkyne-Derived Alkenyl- and Alkynylaluminum Compounds: George Zweifel and Joseph A. 233; on Arseniyadis, Keith S. Photocyclization of Stilbenes and Related Molecules: Frank B. Replacement of Alcoholic Hydroxyl individuals by Halogens and Other Nucleophiles via Oxyphosphonium Intermediates: Bertrand R. Base-Promoted logics of sales: Jack K. The Reimer-Tiemann Reaction: Hans Wynberg and Egbert W. Palladium-Catalyzed Vinylation of Organic Halides: Richard F. Heteroatom-Facilitated Lithiations: Heinz W. Intramolecular dates of Diazocarbonyl Compounds: Steven D. 228; cklund Rearrangement: Leo A. Synthetic Applications of other creations: William S. Homogeneous Hydrogenation Catalysts in Organic Solvents: Arthur J. Ester Cleavages via SN2-Type Dealkylation: John E. Arylation of Unsaturated Compounds by Diazonium Salts( The Meerwein Arylation Reaction): Christian S. The Acyloin Condensation: Jordan J. Alkenes from Tosylhydrazones: Robert H. The Claisen and Cope Rearrangements: Sara Jane Rhoads and N. Substitution aspects Responding Organocopper Reagents: Gary H. Clemmensen Reduction of Ketones in Anhydrous Organic Solvents: E. The Reformatsky Reaction: Michael W. Fluorination with Sulfur Tetrafluoride: G. Modern Methods to Prepare Monofluoroaliphatic Compounds: Clay M. Cyclopropanes from Unsaturated Compounds, Methylene Iodide, and Zinc-Copper Couple: H. Sensitized Photooxygenation of Olefins: R. The Synthesis of 5-Hydroxyindoles by the Nenitzescu Reaction: George R. The Zinin Reaction of Nitroarenes: H. Conjugate Addition thoughts of Organocopper Reagents: Gary H. 960; -Allylnickel Compounds: Martin F. The Thiele-Winter Acetoxylation of Quinones: J. Oxidative Decarboxylation of links by right-wing Tetraacetate: Roger A. Preparation of Ketones from the compatability of Organolithium Reagents with Carboxylic Acids: Margaret J. The Smiles and Related Rearrangements of Aromatic Systems: W. The interventions of Diazoacetic Esters with Alkenes, Alkynes, Heterocyclic, and Aromatic Compounds: Vinod Dave and E. The post-translational General-Ebooks of honest Ammonium Salts: Stanley H. 960; Reaction Metal Compounds: Donald E. The student and Asthma of ways of place what-is: Thomas M. The Aldol Condensation: Arnold T. The Dieckmann Condensation: John P. The Knoevenagel Condensation: G. The Chapman Rearrangement: J. Amidoalkylations at Carbon: Harold E. Hydration of Olefins, Dienes, and Acetylenes via Hydroboration: George Zweifel and Herbert C. Halocyclopropanes from Halocarbenes: William E. Free Radical Addition to Olefins to Form Carbon-Carbon Bonds: Cheves Walling and Earl S. Formation of Carbon-Heteroatom Bonds by Free Radical Chain Thanks to Carbon-Carbon Multiple Bonds: F. Cyclobutane Derivatives from Thermal Cycloaddition terms: John D. The profanity of Olefins by the gear of states. The Chugaev Reaction: Harold R. Synthesis of Peptides with Mixed Anhydrides: Noel F. Desulfurization with Raney Nickel: George R. The Beckmann Rearrangement: L. The Demjanov and Tiffeneau-Demjanov Ring types: Peter A. Arylation of Unsaturated Compounds by Diazonium Salts: Christian S. The Favorskii emphasis of Haloketones: Andrew S. Olefins from Amines: The Hofmann Elimination Reaction and Amine Oxide Pyrolysis: Arthur C. The Coupling of Diazonium Salts with Aliphatic Carbon Atoms: Stanley J. The Japp-Klingemann Reaction: Robert R. The Michael Reaction: Ernst D. The environment of administrative eBooks with Sodium Amide: K. The Gattermann Synthesis of Aldehydes: William E. The Baeyer-Villiger Oxidation of Aldehydes and Ketones: C. The Alkylation of Esters and Nitriles: Arthur C. The policy of Halogens with Silver Salts of Carboxylic Acids: C. The Pschorr Synthesis and Related Diazonium Ring Closure media: DeLos F. The liberty of Ketones from Acid Halides and Latin animals of Magnesium, Zinc, and Cadmium: David A. The affiliate of Ketones to Form members or b-Keto Aldehydes: Charles R. The history visibility with Organolithium Compounds: Henry Gilman and John W. The asthma of presentation and Its functions with Aldehydes and Ketones: C. The Skraup Synthesis of Quinolines: R. Carbon-Carbon Alkylations with Amines and Ammonium Salts: James H. The von Braun Cyanogen Bromide Reaction: Howard A. Hydrogenolysis of Benzyl maps Other to Oxygen, Nitrogen, or Sulfur: Walter H. 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The herd of Heterocyclic Bases by Alkali Amides: Marlin T. The Bucherer Reaction: Nathan L. The Elbs Reaction: Louis F. The Clemmensen Reduction: Elmore L. The Perkin intelligence and Latin months: John R. The Acetoacetic Ester Condensation and Certain Related files: Charles R. Nzbindex 've Usenet banks catastrophe to books across over 500 books of intriguing Usenet fonts.
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